FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

PERMARIDGE SYRINGE

K Number: K962838 · Decision Aug 20, 1996
Classifications
1
FEI Numbers
97
Registration Numbers
97
Same Product Code
225
Applicant Total
16
Review Days
29

Basic Information

Device Name
PERMARIDGE SYRINGE
K Number
K962838
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3930
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
CERAMED CORP.
Date Received
July 22, 1996
Decision Date
August 20, 1996
Product Code
LYC
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LYC Bone Grafting Material, Synthetic

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LYC), ordered by most recent decision date.

View all

Other Clearances by CERAMED CORP.

K Number Device Name
K962786 OSTEOGRAF STAINLESS STEEL SYRING
K960348 OSTEOGRAF/N-300 HYDROXYLAPATITE
K960368 OSTEOGRAFT/N-700 HYDROXYLAPTITE
K960353 OSTEOGRAF/LD-300 HYDROXYLAPATITE
K960361 PERMAMESH-D HYDROXYLAPATITE MATRIX
K960362 PERMAMESH HYDROXYLAPATITE MATRIX
K960354 PERMAMESH-D HYDROXYLAPATITE MATRIX
K960349 PERMARIDGE HYDROXYLAPATITE MATRIX
K954631 OSTEOGRAF/N-BLOCCK HYDROXYLAPATITE
K942946 OSTEOGRAF/D-100 HYDROXYLAPATITE
Search all 16 clearances from CERAMED CORP. →